Biotech CQV Scheduler - Lead Validation Timelines (Onsite)

A trusted consulting partner in Norwood, MA, is seeking a CQV Project Scheduler to coordinate and oversee CQV activities at a biotechnology manufacturing site. This is a 6-month onsite contract where you'll blend technical expertise with project scheduling. Ideal candidates have 5+ years of experience in CQV and biotech facility startup. Proficiency in project management tools like Smartsheet is required. Engagement may be structured as either W-2 or 1099, with competitive hourly compensation. #J-18808-Ljbffr